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BioWorld - Saturday, July 25, 2026
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Regulatory front

July 11, 2019
The Institute for Clinical and Economic Review (ICER) unveiled its preliminary list of potential assessment topics for next year. The list is based on the projected timing and likelihood of FDA approval, and whether an evidence review would suggest specific actions for payers, physicians, patients and policymakers to improve clinical practice. 
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Regulatory front

July 10, 2019
The World Health Organization (WHO) Tuesday updated its list of essential medicines, with a focus on cancer and other global health challenges. WHO added 28 drugs for adults and 23 for children to the medicines list and specified new uses for 26 drugs already on the list. 
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Regulatory front

July 9, 2019
The U.S. Court of Appeals for the Federal Circuit Friday unsealed its decision in the patent lawsuit between Enzo Life Sciences Inc. and a group of defendant-appellees led by Roche Molecular Systems Inc., affirming a lower court's decision to grant summary judgment against Enzo for lack of enablement of the disputed patent claims. 
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Focus V approved in China for soft tissue sarcoma

July 8, 2019

FDA approves Xembify for primary immunodeficiencies

July 5, 2019

Regulatory front

July 5, 2019
In an ongoing crackdown on repackers, the FDA recently issued warning letters to three repackers of active pharmaceutical ingredients (API) for significant violations of current good manufacturing practice requirements.
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FDA grants accelerated approval to Xpovio for relapsed refractory multiple myeloma

July 4, 2019

FDA warning letters decline under Trump, inspections increase

July 3, 2019
By Mari Serebrov
The FDA's Center for Drug Evaluation and Research (CDER) issued 62% more warning letters under the first part of the Trump administration than it did during the last few years of the Obama administration. But the number of warnings for medical devices, food and tobacco products fell sharply under President Donald Trump, according to an investigative report being published in the July 5 issue of Science.
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Regulatory front

July 2, 2019
The FDA Monday released two draft guidances on the content and format of specific sections in prescription drug labeling. 
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Danish Medicines Agency approves AJ Vaccines' polio vaccine

July 1, 2019
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